Integra LifeSciences Corporation
Integra LifeSciences Corporation sponsors 60 registered US clinical trials on ClinicalTrials.gov, 3 of them currently recruiting, and 38 completed. 5 of these trials are in Phase 3-4 (later-stage) and 1 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Diabetic Foot Ulcer, with 2 trials.
Trial Pipeline
60 total, page 1 of 2
AERA Pediatrics Registry
NCT07071298
A Modified Platform Trial of Multiple CAMPs for the Management of Diabetic Foot Ulcers and Venous Leg Ulcers
NCT06453187
The MIRROR Registry: Minimally Invasive IntRaceRebral HemORrhage Evacuation
NCT04494295
MicroMatrix® Flex in Tunneling Wounds
NCT06629506
Cavitronic Ultrasonic Surgical Aspiration (CUSA) Women's Health Study
NCT06297187
T-GENVIH-003 LTFU (Long Term Follow Up) Study
NCT06034652
Gentrix® Surgical Matrix for Soft Tissue Reinforcement in Ventral Hernia Repair
NCT05610267
REINVENT Registry (Registry of the Nerve Gap Repair From Integra)
NCT05339594
NeuraGen 3D Pilot Study
NCT05343143
The Purpose of This Study is to Determine Whether CerebroFlo™ EVD Catheter is Effective During the Treatment of Intraventricular Hemorrhage (IVH)
NCT05113381
Suturable DuraGen™ PMCF Study
NCT04923867
Diabetic Foot Ulcer Study Comparing Cytal Wound Matrix 1-Layer to Standard of Care
NCT03626623
Sundt™ Carotid Shunt Retrospective Post Market Clinical Follow-up Study (PMCF)
NCT03816202
The Management of Pilonidal Wounds With ACell MicroMatrix® and Cytal® Wound Matrix: A Case Series
NCT04041037
Cytal® Wound Matrix and MicroMatrix® Wound Study
NCT03632954
AMNIOEXCEL® Plus vs A Marketed Comparator vs SOC in the Management of Diabetic Foot Ulcers
NCT03547635
Comparing Concomitant Use of ACell MicroMatrix® and ACell Cytal™ to Standard of Care in Stage 3 or 4 Pressure Injuries
NCT03283787
PriMatrix for the Management of Diabetic Foot Ulcers
NCT03010319
Open-Label Study in Diabetic Foot Ulcers (DFU), to Evaluate Safety of 0.03% DSC127 Topical Gel in Chronic Use
NCT01840085
MEDIHONEY® Gel Versus Collagenase for Wound Debridement
NCT02482948
Global Sinus Surgery Registry
NCT02347943
Phase IV Study to Evaluate the Efficacy of AMNIOEXCEL in Diabetic Foot Ulcers
NCT02209051
ACell MatriStem Pelvic Floor Matrix Versus Native Tissue Repair, Comparative Study
NCT02021279
Study of Safety and Efficacy for the Eustachian Tube Balloon Catheter
NCT02087150
Retrospective Study Evaluating Outcomes for Integra® Skin Sheet Products in Lower Extremity Complex Wounds
NCT01947387
A Comparative Efficacy Study: Treatment for Non-healing Diabetic Foot Ulcers
NCT01858545
Phase 3 Study Evaluating Efficacy and Safety of DSC127 Compared With Vehicle and With Standard-of-care in Diabetic Foot Ulcers
NCT01849965
Phase III Study to Evaluate Efficacy and Safety of DSC127 in Diabetic Foot Ulcers
NCT01830348
Comparison of Balloon Sinuplasty In-Office Versus Medical Management for Recurrent Acute Sinusitis Patients (CABERNET)
NCT01714687
Medical Therapy Versus Balloon Sinus Dilation for Patients With Chronic Rhinosinusitis
NCT01685229
Health Economic Assessment of Lower Extremity Diabetic (HEALED) Ulcers With PriMatrix
NCT01729286
Earset Healthy Volunteer Study
NCT01611246
Tympanostomy Tube Placement in Children in the Office (Inova Study)
NCT01496287
inVENT-visIOn Study
NCT01444391
DuraSeal Exact Spine Sealant System Post-Approval Study
NCT01410864
Healthy Volunteer Study
NCT01346332
inVENT-In-Office Study
NCT01324271
A Study With Primatrix Dermal Repair Scaffold For The Treatment Of Diabetic Foot Ulcers
NCT01270633
Evaluation of the Tympanostomy Tube Delivery System
NCT01202578
A Multicenter, Prospective, Observational Study With PriMatrix for the Treatment of Neuropathic Diabetic Foot Ulcers
NCT01228526
Optimization and Refinement of Technique in In-Office Sinus Dilation 2
NCT01107379
A Safety and Efficacy Study of INTEGRA® Dermal Regeneration Template for the Treatment of Diabetic Foot Ulcers
NCT01060670
Acclarent Tympanostomy Tube Delivery System for the Treatment of Patients Requiring Tympanostomy Tube Insertion
NCT02150044
An Evaluation of SprayShield in Reducing Post-Operative Adhesion Formation Following Major Open Abdominal Surgery
NCT01002287
Anesthetizing the Tympanic Membrane in Healthy Volunteers
NCT01047904
Large Abdominal Hernia Repair With SurgiMend 3.0
NCT00892333
Clinical Study of the Tympanostomy Tube Delivery System
NCT00939796
Clinical Study of Safety and Efficacy for the Relieva Stratus With Elution of Triamcinolone Acetonide
NCT00791934
PleuraSeal Pivotal Study (US)
NCT00748124
Balloon Sinus Dilation In Office or OR
NCT00939393
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 2 | 1 |
| Phase 3 | 4 |
| Phase 4 | 1 |
Therapeutic Areas
What the Pipeline for Integra LifeSciences Corporation Shows
According to the ClinicalTrials.gov registry, Integra LifeSciences Corporation is linked to 60 US clinical trials across every stage of research activity. Of those, 3 studies are currently recruiting, about 5% of the sponsor's indexed portfolio, and 38 are already marked complete, representing roughly 63% of the total.
The phase mix for Integra LifeSciences Corporation reports 5 late-stage studies (Phase 3 and Phase 4 combined) and 1 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Integra LifeSciences Corporation is Diabetic Foot Ulcer with 2 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.